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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037564Generated: October 30, 2026

Cesium carbonate → 6-(3-aminophenyl)-2-(4-fluorophenyl)-N-methyl-2H-indazole-3-carboxamide

https://huagongshe.com/reaction/1037564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBoronic AcidHCID 61668—
Reactant6-bromo-2-(4-fluorophenyl)-N-methyl-2H-indazole-3-carboxamideHCID 67775673—
CatalystHCID 178418397HCID 178418397—
SolventEthanolHCID 702—
Product6-(3-aminophenyl)-2-(4-fluorophenyl)-N-methyl-2H-indazole-3-carboxamideHCID 56962926222%

Reaction Conditions

Temperature8 °C

Reaction Steps

A suspension of compound (xvii) (10 mg, 0.03 mmol), boronic acid (5.9 mg, 0.04 mmol), cesium carbonate (14 mg, 0.04 mmol) and tetrakis(triphenylphosphine)palladium (2 mg, 0.001 mmol) in ethanol (2 mL) were degassed and stirred under an atmosphere of nitrogen then heated to 8° C. After 3 h the reaction mixture was concentrated and the residue was partitioned between EtOAc (25 mL) and water (15 mL). The organic layer was separated and the aqueous layer was extracted with EtOAc (3×15 mL). The combined organics were washed with brine (15 mL), dried (MgSO4) and concentrated to give 6-(3-aminophenyl)-2-(4-fluorophenyl)-N-methyl-2H-indazole-3-carboxamide (16) (12 mg) as a pale brown oil. The crude material was used directly. ESI-MS m/z calculated for [M+H]+: 361.13; found: 361.14.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546389B2
Source datasetuspto-grants-2013_10
ORD IDord-4538c039bd16469d8c7ac3202aa872d6
Source noteuspto-grants-2013_10